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Hydrochloric Acid → 2-Chloro-4-methyl-5-(4-nitro-phenyl)-thiazole

HRID 908154
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HRID 908154 반응식
N(OCCC(C)C)=O.[CH3:9][C:10]1[N:11]=[C:12](N)[S:13][C:14]=1[C:15]1[CH:20]=[CH:19][C:18]([N+:21]([O-:23])=[O:22])=[CH:17][CH:16]=1.[ClH:25]>CC#N.[Cu](Cl)Cl>[Cl:25][C:12]1[S:13][C:14]([C:15]2[CH:20]=[CH:19][C:18]([N+:21]([O-:23])=[O:22])=[CH:17][CH:16]=2)=[C:10]([CH3:9])[N:11]=1
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참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 8053Isoamyl NitriteHCID 6166034-Methyl-5-(p-nitrophenyl)-2-thiazolamine

생성물 1

HCID 673914002-Chloro-4-methyl-5-(4-nitro-phenyl)-thiazole

시약·촉매·용매 2

HCID 24014Cupric Chloride촉매HCID 6342Acetonitrile용매

실험 절차

Isoamyl nitrite (3.5 ml, 25 mmol) is added to a stirred suspension/solution of anhydrous copper (II) chloride (2.75 g, 20 mmol) in dry methylcyanide (50 ml). 4-Methyl-5-(4-nitro-phenyl)-thiazol-2-ylamine (25a) (4.0 g, 17 mmol) is then added over 30 minutes. The resulting slurry is stirred at room temperature for 1 hour then heated at 70° C. for 30 minutes. After cooling to room temperature the black solution is poured into 4M hydrochloric acid (200 ml). The product is extracted with ethyl acetate, dried (MgSO4) and the solvent removed to give the title compound as an orange powder (3.13 g). MH+ (TOF, ES+): 255.0

후처리

  1. temperaturethen heated at 70° C. for 30 minutes
  2. temperatureAfter cooling to room temperature the black solution
  3. extractionThe product is extracted with ethyl acetate
  4. dry with materialdried (MgSO4)
  5. customthe solvent removed

출처 및 근거

ORD 기록
ord-3e0dd559dc45408d914484da96d8f166
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08017608B2

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